circRNA basic information
circBase ID: hsa_circ_0004277
Name: -
Synonym: -
Host Gene: -
Genomic location(hg19): chr10:1125950-1126416:+
Genomic location(hg38): chr10:1080010-1080476:+
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005084
MONDO name: mental disorder
Disease details: psychological distress
Disease DO ID:
-
Disease MeSH ID:
-
Disease NCIt ID:
-
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

blood; peripheral blood mononuclear cells

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: BRCA1
Associated microRNA: hsa-miR-1287-5p, hsa-miR-1343-3p, hsa-miR-148b-5p, hsa-miR-181a-3p, hsa-miR-191-5p, hsa-miR-193b-3p, hsa-miR-330-5p, hsa-miR-582-3p, hsa-miR-92b-3p, hsa-miR-24-3p
Biological function: May influence the pathophysiological processes of psychological distress in NPC patients receiving radiotherapy.
Molecular mechanism: Putative ceRNA mechanism via hsa-miR-24-3p and hsa-miR-92b-3p regulating BRCA1 within a constructed ceRNA network.
Biological pathway or process:

ceRNA regulation (other)

Detected method:
Q
S
Validation methods:

RNA-seq; RT-qPCR; Clinical Sample Validation; Bioinformatics Analysis

Clinical significance:

Significant expression differences between rise and decline distress groups during radiotherapy (potential genetic factor for PD trajectories).

Description:

hsa_circ_0004277 is higher in the rise-distress trajectory than in the decline-distress trajectory in NPC patients during radiotherapy (blood/ PBMC samples). The study proposes a ceRNA mechanism involving hsa-miR-24-3p or hsa-miR-92b-3p regulating BRCA1, potentially contributing to PD-related pathophysiology.

Confidence score:

0.4032

Other information
Title:

Trajectories and influencing factors of psychological distress in nasopharyngeal carcinoma patients receiving radiotherapy (incorporating genetic factors): a multicenter longitudinal study.

Journal: Frontiers in oncology
Published: 2025
PubMed ID: 40936698
Study type:

combined biological and clinical study

Data availability: GEO database ()
Code availability: -